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Homoallyl ethers regioselective oxidation

Oxidation of allylic andhomallylic acetates (cf. 10,175-176).1 This system is an efficient catalyst for oxygenation of terminal alkenes to methyl ketones (Wacker process). Similar oxidation of internal olefins is not useful because it is not regioselective. However, this catalyst effects oxygenation of allylic ethers and acetates regioselectively to give the corresponding /i-alkoxy ketones in 40-75% yield. Under the same conditions, homoallylic acetates are oxidized to y-acetoxy ketones as the major products. [Pg.203]

Regioselective Oxidation Allyl and Homoallyl Ethers and Esters... [Pg.449]

Allyllic ether 53 is oxidized regioselectively to the /3-alkoxy ketone 54, which is converted into the a,/i-unsaturated ketone 55 and used for annulation[99]. The ester of homoallylic alcohol 56 is oxidized mainlv to the 7-acetoxy ketone 57[99]. [Pg.28]


See other pages where Homoallyl ethers regioselective oxidation is mentioned: [Pg.474]    [Pg.375]    [Pg.243]    [Pg.410]    [Pg.319]    [Pg.1044]   
See also in sourсe #XX -- [ Pg.464 ]

See also in sourсe #XX -- [ Pg.464 ]

See also in sourсe #XX -- [ Pg.7 , Pg.464 ]

See also in sourсe #XX -- [ Pg.7 , Pg.464 ]

See also in sourсe #XX -- [ Pg.464 ]




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Ethers oxidation

Homoallyl

Homoallylation

Homoallylic

Homoallylic ethers

Oxidation regioselective

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